A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6983956



Internal ID12977441
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:136665653..136898857hg38UCSC Ensembl
Innerchr8:137677896..137911100hg19UCSC Ensembl
Innerchr8:137747078..137980282hg18UCSC Ensembl
Innerchr8:137747078..137980282hg17UCSC Ensembl
Cytoband8q24.23
Allele length
AssemblyAllele length
hg38233205
hg19233205
hg18233205
hg17233205
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2752222
Supporting Variants
SamplesBEC_737
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6983956
Frequency
Sample Size771
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer